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NCT01680055 Clinical Trial

Collection of Blood and Bone Marrow From Patients With Aplastic Anemia for Analysis of Adhesion Molecules, Chemokines and Their Receptors

Healthy Clinical Trial

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT01680055
Other study ID # Aplastic Anemia 1
Secondary ID
Status Withdrawn
Phase N/A
First received September 3, 2012
Last updated April 18, 2016
Start date February 2009
Est. completion date November 2012

Study information
Verified date September 2012
Source Shandong University
Contact n/a
Is FDA regulated No
Health authority China: National Natural Science Foundation
Study type Observational

Clinical Trial Summary

This study is designed to collect bone marrow and/or peripheral blood cells and plasma, for the analysis of adhesion molecules, chemokines and their receptors from newly-diagnosed aplastic anemia patients, and patients treated with antithymocyte globulin plus cyclosporine

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date November 2012
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 16 Years to 70 Years
Eligibility Inclusion Criteria:

- patients who fulfilled entry criteria of acquired aplastic anemia age range 16-70 years

Exclusion Criteria:

- Patients complicated with diabetes, tumor, pregnancy, active infection, or connective tissue diseases, such as systemic lupus erythematosus.

Study Design

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
China Qilu Hospital, Shandong University Jinan Shandong

Sponsors (1)
Lead Sponsor Collaborator
Shandong University

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary hematologic response hematologic response at 6 months following antithymocyte globulin plus cyclosporine treatment, defined as no longer meeting the criteria for severe aplastic anemia 6 months following antithymocyte globulin plus cyclosporine treatment No
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